Case ReportL-V. M. is a 42-year-old man with unknown medical history except for obesity and an excessive consumption of alcohol and derived. He has come to our attention for a persistent fever, higher than 38°C, with chills, mainly but not exclusively in the evening, that lasted for more than 3 weeks. It was not associated with specific organ symptoms and in his past and recent medical history there were no clues to suspect a specific etiology, according to the most recent literature.1 No consumption of any drugs, over-the-counter products or narcotic substances were reported.Previously investigated at another hospital, the fever was associated with significant and persistent increases in enzymes of hepatic cytolisis and cholestasis (Table 1); serological investigations proved positive exclusively for rheumatoid factor (RF) and antismooth muscle antibodies (ASMA). The fever was responsive to a first antibiotic course with ceftriaxone (7 days) and to a following second antibiotic course with piperacillin-tazobactam (5 days), administered in two previous admissions. In both situations, there was a complete resolution of the fever followed by a new recurrence of the symptoms. The abdominal ultrasonography and abdominal magnetic resonance imaging/magnetic resonance cholangiography showed a picture of hepatic steatosis, without further morphological alterations.In our division, we confirmed the known defects of hepatic cytolisis and cholestasis; we found a significant increase in C-reactive protein in the absence of leukocytosis and of procalcitonin increase. Lymphocytes immunophenotyping was negative. Regarding autoimmunity, we found a positive low title for RF, lupus anticoagulant and anticardiolipin antibodies. We broadened our serological investigations with the observation of positive low title for Widal Wright reaction. The standard cultures (three sets of blood culture, urine culture, culture of sputum with special search for mycobacterium and oropharyngeal swab) were all negative. A chest X-ray and an echocardiogram were negative for pleuro-parenchymal lesions and for endocardial vegetations or masses. Our final diagnostic test was a liver biopsy.While waiting for the histological result, we started steroid therapy (dosage 1 mg/kg) in the suspect of an autoimmune disease. We got a full and stable defervescence, but only a partial reduction in hepatic enzymes of cytolisis and cholestasis and in C-reactive protein (Table 1). After two weeks we got the result of liver biopsy that reported the presence of steatosis with a severe lipogranulomatosis, with the indications to carry out further investigations in the setting of acquired diseases, above all infectious diseases.We performed additional microbiological tests, in-
ABSTRACTQ fever is an infectious disease caused by Coxiella burnetii. Its clinical presentation is often nonspecific and the serological diagnosis difficult to make, especially in the absence of specific and suspected medical history. This article presents a case of fever of unknown origin (FUO),...